Sales Edijane M, Sousa Gileno S, Belouezzane Chiraz, Almeida Fábio C L, Figueroa-Villar José D
Instituto Militar de Engenharia, Departamento de Química, 22290-270, Brazil.
Instituto de Bioquímica Médica, Centro Nacional de Ressonância Magnética Nuclear Jiri Jonas, Universidade Federal do Rio de Janeiro, 21941-920, Brazil.
Protein Expr Purif. 2019 Sep;161:40-48. doi: 10.1016/j.pep.2019.04.009. Epub 2019 Apr 27.
Leishmaniasis represents an important public health problem in several countries. The main target in this study is the nucleoside hydrolase Leishmania chagasi (LcNH) that is responsible for causing visceral leishmaniasis, principally in Brazil. Nucleoside hydrolase enzymes are members of this pathway, hydrolyzing the N-glycosidic bond of ribonucleosides for the synthesis of nucleic acids. We present here for the first time, the expression and purification protocols to obtain the enzymes LcNH1 and LcNH2 that can be employed to explore novel strategies to produce nucleoside hydrolase inhibitors for use in chemotherapy. Protein integrity was also confirmed by SDS-PAGE gel, mass spectrometry and enzymatic activity.
利什曼病在多个国家是一个重要的公共卫生问题。本研究的主要目标是核苷水解酶恰加斯利什曼原虫(LcNH),它是导致内脏利什曼病的原因,主要在巴西。核苷水解酶是该途径的成员,可水解核糖核苷的N-糖苷键以合成核酸。我们在此首次展示了获得LcNH1和LcNH2酶的表达和纯化方案,这些酶可用于探索生产用于化疗的核苷水解酶抑制剂的新策略。还通过SDS-PAGE凝胶、质谱和酶活性确认了蛋白质的完整性。